Chronisense Medical, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Chronisense Medical, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Polso Watch
1
Total
1
Cleared
0
Denied
Chronisense Medical, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Yokneam Illit, IL.
Last cleared in 2022. Active since 2022. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Chronisense Medical, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by RQM+ as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Chronisense Medical, Ltd.
1 devices